Ethereal monosubstitutions of monosaccharide derivatives

ABSTRACT

The invention provides a novel therapeutic composition comprising a pharmaceutically acceptable carrier containing a therapeutically effective amount of an ethereal monosubstitution of a monosaccharide derivative having the general formula S--O--Y, wherein S is the residue of the monosaccharide derivative selected from the group consisting of pentoses, hexoses and heptoses as single or polysubstituted acetals, ketals or esters and Y is selected from the group consisting of cyclic monovalent nitrogen-containing organic radicals and residua and monovalent organic radicals and residua having the general formula ##STR1## wherein R 1  is a divalent organic radical having a linear carbon chain length of about 1-7 carbon atoms and R 2  and R 3  are selected from the group consisting of --H, --OH, --SH, halogen and monovalent organic radicals and residua having a linear carbon chain length of about 1-7 carbon atoms. The invention also provides certain novel ethereal monosubstitutions of monosaccharide derivatives, of which 3-O-3&#39;-(N&#39;,N&#39;-dimethylamino-n-propyl)-1,2-O-isopropylidene-D-glucofuranose is an example. The novel monosaccharide derivatives show striking antiviral activity or other therapeutically valuable properties and are useful as active ingredients in the above therapeutic composition. The invention further provides a method of therapeutically treating warm-blooded animals with the aforementioned therapeutic composition and novel monosubstituted monosaccharide derivatives.

RELATED APPLICATION

This application is a continuation in part of my copending application Ser. No. 337,134, filed on Mar. 1, 1973, .Iadd.now U.S. Pat. No. 3,939,145 .Iaddend.for Therapeutic Composition, Novel Compounds Useful Therein and Method of Using the Same.

BACKGROUND OF THE INVENTION

The present invention is concerned with a novel therapeutic composition and a method of therapeutically treating warm-blooded animals therewith. In one of its more specific variants, the invention further relates to certain novel ethereal monosubstitutions of monosaccharide derivatives which are especially useful as ingredients in the aforementioned compositions and in practicing the aforementioned method.

Many diseases caused by certain living microorganisms may be treated very effectively by administering a therapeutically effective amount of an antibiotic. However, antibiotics are not effective in the treatment of virus infections insofar as suppressing the proliferation of the virus particles and reducing cell damage are concerned.

A number of substances other than antibiotics have been proposed heretofore for use in treating virus infections, but they have not been used extensively for a number of reasons. For instance, the previously proposed antiviral agents usually exhibit very low antiviral activity and have little positive effect on the course of the viral infection. The previously proposed antiviral drugs also have not been effective in the treatment of a wide spectrum of virus infections and this has been a major disadvantage. The therapeutic treatment of a large number of patients having undetermined viral infections of widely differing types is impractical with the narrow spectrum prior art antiviral drugs, as it is too difficult to determine the exact virus causing the infection and then select an effective drug. Many potentially effective antiviral drugs are toxic and cannot be safely administered to patients, and still other antiviral drugs have undesirable side effects. As a result of the foregoing and other deficiencies, it is apparent that an entirely satisfactory wide spectrum nontoxic antiviral drug has not been available heretofore for routinely administering to patients having a viral infection caused by many of the common viruses.

It has been discovered that certain ethereal monosubstitutions of monosaccharide derivatives provide important biological signals which allow living cells to resist virus infections. As will be described in greater detail hereinafter, the signals also provide other types of control in cell chemistry.

The therapeutic compositions of the invention overcome the disadvantages of the prior art antiviral agents noted above, and also produce other unusual and unexpected results. For example, the ethereal monosubstitutions of monosaccharide derivatives described hereinafter are therapeutically effective at very low concentrations, while at the same time they exhibit no side effects and are very nontoxic. The ratio of the minimum toxic to therapeutic dose is greater than 50 in both tissue culture and animals.

The antiviral compounds and the therapeutic compositions containing the same disclosed and claimed in my earlier filed copending application Ser. No. 337,134 possess striking antiviral properties and are highly effective in the treatment of a wide variety of viral infections in warm blooded animals. Nevertheless, the earlier described antiviral compounds and therapeutic composition do have certan limitations and disadvantages which are over come by the present invention. For example, the earlier described compounds possess strong hydrophilic properties due to the presence of a plurality of free hydroxyl groups which result in several limitations on the effective use thereof in situ including short shelf life, variability of the stability in solution as a function of temperature, and extreme hygroscopicity.

The compounds of the present invention have been found to be more desirable with respect to the properties listed above. This is presently believed to be the direct result of a decrease in the hydrophilic properties and, thereby, an increase in the solubility of the compounds in the fatty tissues of a warm-blooded animal which has been therapeutically treated therewith. This technique also aids in the transportation of the drug to a desired tissue or the concentration thereof in a desired tissue. In the practice of one variant of the invention, an organic substituent is selected which blocks at least one free monosaccharide hydroxyl group and thereby decreases the hydrophilic properties and allows the compound to be transported or concentrated in fatty tissues. In a further variant, a labile organic substituent is selected which may be removed in vivo during treatment of the warm-blooded animal after it has served its purpose, thereby unblocking the hydroxyl group (s).

It is an object of the present invention to provide a therapeutic composition including a pharmaceutically acceptable carrier and a therapeutically effective amount of certain ethereal monosubstitutions of monosaccharide derivatives to be described more fully hereinafter.

It is a further object to provide certain novel compounds to be described more fully hereinafter, which are ethereal monosubstitutions of monosaccharide derivatives exhibiting striking antiviral activity and/or other therapeutically valuable properties.

It is still a further object to provide a therapeutic composition containing one or more of the novel monosaccharide derivatives of the invention.

It is still a further object to provide a method of therapeutically treating a warm-blooded animal wherein the above described therapeutic composition and/or novel monosaccharide derivatives are administered thereto in a therapeutically effective amount.

Still other objects and advantages of the invention will be apparent to those skilled in the art upon reference to the following detailed description.

DETAILED DESCRIPTION OF THE INVENTION INCLUDING PREFERRED VARIANTS THEREOF

The novel therapeutic composition of the invention comprises a pharmaceutically acceptable carrier and a therapeutically effective amount of an ethereal monosubstitution of a monosaccharide derivative having the general formula S--O--Y and organic and inorganic acid salts thereof, wherein S is the residue of a monosaccharide selected from the group consisting of pentoses, hexoses and heptoses which has been derivatized with (a) one or more aliphatic alcohols containing 1-18 carbon atoms and preferably 1-4 carbon atoms to produce an acetal group at one or more available hydroxyl residua, (b) one or more aldehydes containing 1-18 carbon atoms and preferably 1-4 carbon atoms to produce single or multiple acetal groups at one or more available hydroxyl residua, (c) one or more ketones containing 1-18 carbon atoms and preferably 1-4 carbon atoms to produce single or multiple ketal groups at one or more available hydroxyl residua, or (d) one or more organic acid residua containing 1-18 carbon atoms and preferably 1-4 carbon atoms to produce ester groups at one or more available hydroxyl residua, and Y is selected from the group consisting of cyclic monovalent nitrogen-containing organic radicals and residua and monovalent organic radicals and residua having the general formula ##STR2## wherein R₁ is a divalent organic radical having a linear carbon chain length of about 1-7 carbon atoms and R₂ and R₃ are selected from the group consisting of --H, --OH, --SH, halogen and monovalent organic radicals and residua having a linear carbon chain length of about 1-7 carbon atoms. When R₂ or R₃ is halogen, the halogen may be F, Cl, Br or I, of which Cl or Br is usually preferred. The organic radical R₁, and R₂ and R₃ when they are organic radicals, may be branched or unbranched linear carbon chains and may be saturated or unsaturated, and, when saturated, the linear and/or branched carbon chains may contain one or more double or triple carbon-to-carbon bonds. The linear and/or branched carbon chains of R₁, R₂ and R₃ may be substituted or unsubstituted and, when substituted, one or more substituents may be present, such as --OH, --SH, halogen (F, Cl, Br and/or I), branched or unbranched and saturated or unsaturated hydrocarbon radicals containing 1-7 and preferably 1-3 carbon atoms, --OR₄ and/or --SR₄ radicals wherein R₄ is a branched or unbranched and saturated or unsaturated hydrocarbon radical containing 1-7 and preferably 1-3 carbon atoms, carboxylic acid residua containing 1-7 and preferably 1-3 carbon atoms, and amino groups and aminohydrocarbon radicals containing 1-7 and preferably 1-3 carbon atoms. Preferably R₁ is a hydrocarbon radical having a linear carbon chain length of 1-3 or 1-4 carbon atoms and R₂ and R₃ are individually selected from the group consisting of hydrogen and/or hydrocarbon radicals having linear carbon chain lengths of 1-3 or 1-4 carbon atoms.

Examples of compounds from which cyclic organic radicals and residua are derived include (a) monovalent nitrogen containing saturated, unsaturated or aromatic carbocyclic compounds containing about 4-8 carbon atoms in the ring and preferably about 5-6 carbon atoms in the ring and at least one nitrogen atom attached thereto or to an organo substituent thereon, (b) heterocyclic organic compounds containing about 3-8 carbon atoms in the ring and at least one ring nitrogen atom and (c) derivatives of the foregoing compounds wherein at least one substituent is present, such as --OH, --SH, halogen (F, Cl, Br and/or I), branched or unbranched and saturated or unsaturated hydrocarbon radicals containing 1-7 and preferably 1-3 carbon atoms, --OR₅ and/or --SR₅ radicals wherein R₅ is a branched or unbranched and saturated or unsaturated hydrocarbon radical containing 1-7 and preferably 1-3 carbon atoms, carbocyclic acid residua containing 1-7 and preferably 1-3 carbon atoms, and amino groups and aminohydrocarbon radicals containing 1-7 and preferably 1-3 carbon atoms.

The derivatized monosaccharide residue S may exist in an open chain or cyclic form having the general formulae: ##STR3## wherein X and Z are H, OH, hydroxyalkyl, alkoxyl and/or alkoxyalkyl containing up to 3 carbon atoms, W is H, alkyl, alkenyl, cyclic alkane or cyclic aromatic containing 1-18 and preferably 1-6 carbon atoms or acyl containing 1-18 and preferably 1-4 carbon atoms, and Y represents the same organic radicals and residua as aforementioned for the general formula S--O--Y. The above general formulae illustrate the various isomers of the pentoses, hexoses and heptoses, the relative spatial configuration of the --H and --OH groups about the ring, and the monosubstitution thereof in accordance with one presently preferred variant of the invention. The hydroxyl or alkoxyl residue of the hemiacetal or hemiketal linkage may assume and α or a β configuration. The compounds of the invention may be in the form of anomers or mixtures of anomers.

The configurations of the various derivatives of isomers of the pentoses, hexoses and heptoses are well known to those skilled in this art and numerous reference books are available on the subject, the teachings of which are incorporated herein by reference. For example, see Textbook of Biochemistry, 4th Edition, by West et al (1966) and the Monosaccharides by Stanek, Cerny, Kocourek and Pacak (1963). The prior art discloses, for example, a total of eight open chain isomers for the reducing hexoses, and an even larger number of open chain isomers for the reducing heptoses. Either the D-series or the L-series of the pentoses, hexoses and heptoses may be used in practicing the invention, but it is usually preferred to use the D-series. The hexoses often give the best results and especially D-talose, D-galactose, L-galactose, D-idose, D-gulose, D-mannose, D-glucose, L-glucose, D-altrose and D-allose. The aforementioned pentoses, hexoses and heptoses may be ethereally monosubstituted in any available position and derivatized at one or more of the remaining hydroxyl groups. Nevertheless, it is understood that substitution of certain positions of specific monosaccharide derivatives results in more therapeutically active or less toxic compounds. For instance, substitution of the 3-O- position of 1,2-O-isopropylidene-D-glucofuranose or 1,2:5,6-di-O-isopropylidene-D-glucofuranose and the 6-O- position of 1,2-O-isopropylidene-D-galactopyranose or 1,2:3,4-di-O-isopropylidene-D-galactopyranose results in especially valuable compounds.

The following substituents may be ethereally substituted on any of the available positions of the various isomers of the pentoses, hexoses and heptoses to produce nontoxic compounds having exceptional therapeutic activity:

-(n-propylamino),

-(N',N'-dimethylamino-n-propyl),

-(N',N'-dimethylaminoisopropyl),

-(N'-methylpiperidyl),

-(N',N'-dimethylaminoethyl),

-(N',N'-diethylaminoethyl),

-(2',N',N'-trimethylamino-n-propyl),

-dimethylamino,

-(N',N'-dimethylaminomethyl),

-(N',N'-dimethylaminopropyl),

-(N',N'-dimethylamino-iso-butyl),

-(N',N'-dimethylamino-n-butyl),

-(N',N'-dimethylamino-iso-pentyl),

-(N',N'-dimethylaminopentyl),

-(N'-methylamino-n-propyl),

-(N'-methyl-N'-ethylamino-n-propyl),

-(N',N'-diethylamino-n-propyl),

-(amino-n-propyl),

-(N'-ethylamino-n-propyl),

-(N'-propylamino-n-propyl),

-(N',N'-iso-propylamino-n-propyl),

-(1',2'-ethylimino-n-propyl),

(1"-n-propylpyrrolidyl),

(1"-n-propylpiperidyl),

-piperidyl,

-(N',N'-dimethylamino-sec-butyl).

Of the foregoing substituents, -(N',N'-dimethylamino-n-propyl) is presently preferred and especially when substituted in the 3-O- position of 1,2-O-isopropylidene-D-glucofuranose or 1,2:5,6-di-O-isopropylidene-D-glucofuranose or the 6-O- position of 1,2-O-isopropylidene-D-galactopyranose or 1,2:3,4-di-O-isopropylidene-D-galactopyranose.

The following compounds have been found to have exceptional wide spectrum antiviral activity and other therapeutically valuable properties and are presently preferred for use in the composition and method of the invention:

3-O-3'-(n-propylamino)-1,2,-O-isopropylidene-D-glucofuranose,

3-O-3'-(N',N'-dimethylamino-n-propyl)-1,2-O-isopropylidene-D-glucofuranose,

3-O-4'-(N-methylpiperidyl)-1,2-O-isopropylidene-D-glucofuranose,

3-O-2'-(N',N'-dimethylaminoethyl)-1,2,-O-isopropylidene-D-glucofuranose,

3-O-2'-(N',N'-diethylaminoethyl)-1,2-O-isopropylidene-D-glucofuranose,

3-O-3'-(2',N',N'-trimethylamino-n-propyl)-1,2-O-isopropylidene-D-glucofuranose,

3-O-2'-(N',N'-dimethylaminopropyl)-1,2-O-isopropylidene-D-glucofuranose,

6-O-3'-(N',N'-dimethylamino-n-propyl)-1,2-O-isopropylidene-D-galactopyranose,

6-O-2'-(N',N'-dimethylaminopropyl)-1,2-O-isopropylidene-D-galactopyranose,

3-O-3'-(n-propylamino)-1,2:5,6-di-O-isopropylidene-D-glucofuranose,

3-O-3'-(N',N'-dimethylamino-n-propyl)-1,2:5,6-di-O-isopropylidene-D-glucofuranose,

3-O-4'-(N'-methylpiperidyl)-1,2:5,6-di-O-isopropylidene-D-glucofuranose,

3-O-2'-(N',N'-dimethylaminoethyl)-1,2:5,6-di-O-isopropylidene-D-glucofuranose,

3-O-2'-(N',N'-diethylaminoethyl-1,2:5,6-di-O-isopropylidene-D-glucofuranose

3-O-3'-(2',N',N'-trimethylamino-n-propyl)-1,2:5,6-di-O-isopropylidene-D-glucofuranose,

3-O-2'-(N',N'-dimethylaminopropyl)-1,2:5,6-di-O-isopropylidene-D-glucofuranose,

6-O-3'-(N',N'-dimethylamino-n-propyl)-1,2:3,4-di-O-isopropylidene-D-galactopyranose,

6-O-2'-(N',N'-dimethylaminopropyl)-1,2:3,4-di-O-isopropylidene-D-galactopyranose, α-N',N'-dimethylamino-iso-propyl-2,3:5,6-di-O-isopropylidene-D-glucofuranoside,

and organic and inorganic acid salts thereof.

Of the foregoing compounds, 3-O-3'-(N',N'-dimethylamino-n-propyl)-1,2-O-isopropylidene-D-glucofuranose is presently preferred.

Additional compounds of the general formula S--O--Y, wherein Y is ##STR4## which may be used in practicing the invention are listed below:

    ______________________________________                                                        Substituent                                                     Monosaccharide Residue                                                                        (Y)                                                             (S)            R.sub.1     R.sub.2  R.sub.3                                    ______________________________________                                         3-O-1,2-O-isopropylidene                                                       D-glucofuranose                                                                               3'-n-propyl H        methyl                                     3-O-1,2-O-isopropylidene                                                       D-glucofuranose                                                                               3'-n-propyl ethyl    "                                          3-O-1,2-O-isopropylidene                                                       D-glucofuranose                                                                               3'-n-propyl H        ethyl                                      3-O-1,2-O-isopropylidene                                                       D-glucofuranose                                                                               2'-iso-propyl                                                                              methyl   methyl                                     3-O-1,2-O-isopropylidene                                                       D-glucofuranose                                                                               3'-1,2-propenyl                                                                            "        "                                          3-O-1,2-O-isopropylidene                                                       D-glucofuranose                                                                               sec.-butyl  "        "                                          3-O-1,2-O-isopropylidene                                                       D-glucofuranose                                                                               3'-butyl    "        "                                          3-O-1,2-O-isopropylidene                                                       D-glucofuranose                                                                               2'-ethyl    H        H                                          3-O-1,2-O-isopropylidene                                                       D-glucofuranose                                                                               methyl      H        H                                          6-O-1,2-O-isopropylidene                                                       D-galatopyranose                                                                              3'-n-propyl H        methyl                                     6-O-1,2-O-isopropylidene                                                       D-galatopyranose                                                                              3'-n-propyl ethyl    "                                          6-O-1,2-O-isopropylidene                                                       D-galatopyranose                                                                              3'-n-propyl H        ethyl                                      6-O-1,2-O-isopropylidene                                                       D-galatopyranose                                                                              3'-1,2-propenyl                                                                            methyl   methyl                                     6-O-1,2-O-isopropylidene                                                       D-galatopyranose                                                                              2'-iso-propyl                                                                              "        "                                          6-O-1,2-O-isopropylidene                                                       D-galatopyranose                                                                              sec.-butyl  "        "                                          6-O-1,2-O-isopropylidene                                                       D-galatopyranose                                                                              3'-butyl    "        "                                          6-O-1,2-O-isopropylidene                                                       D-galatopyranose                                                                              2'-ethyl    H        H                                          6-O-1,2-O-isopropylidene                                                       D-galatopyranose                                                                              methyl      H        H                                          3-O-1,2:5,6-di-O-iso-                                                          propylidene-D-gluco-                                                           furanose       3'-n-propyl H        methyl                                     3-O-1,2:5,6-di-O-iso-                                                          propylidene-D-gluco-                                                           furanose       3'-n-propyl ethyl    "                                          3-O-1,2:5,6-di-O-iso-                                                          propylidene-D-gluco-                                                           furanose       3'-n-propyl H        ethyl                                      3-O-1,2:5,6-di-O-iso-                                                          propylidene-D-gluco-                                                           furanose       2'-iso-propyl                                                                              methyl   methyl                                     3-O-1,2:5,6-di-O-iso-                                                          propylidene-D-gluco-                                                           furanose       3'-1,2-propenyl                                                                            "        "                                          3-O-1,2:5,6-di-O-iso-                                                          propylidene-D-gluco-                                                           furanose       sec.-butyl  "        "                                          3-O-1,2:5,6-di-O-iso-                                                          propylidene-D-gluco-                                                           furanose       3'-butyl    "        "                                          3-O-1,2:5,6-di-O-iso-                                                          propylidene-D-gluco-                                                           furanose       2'-ethyl    H        H                                          3-O-1,2:5,6-di-O-iso-                                                          propylidene-D-gluco-                                                           furanose       methyl      H        H                                          6-O-1,2:3,4-di-O-iso-                                                          propylidene-D-                                                                 galatopyranose 3'-n-propyl H        methyl                                     6-O-1,2:3,4-di-O-iso-                                                          propylidene-D-                                                                 galatopyranose 3'-n-propyl ethyl    "                                          6-O-1,2:3,4-di-O-iso-                                                          propylidene-D-                                                                 galatopyranose 3'-n-propyl H        ethyl                                      6-O-1,2:3,4-di-O-iso-                                                          propylidene-D-                                                                 galatopyranose 3'-1,2-propenyl                                                                            methyl   methyl                                     6-O-1,2:3,4-di-O-iso-                                                          propylidene-D-                                                                 galatopyranose 3'-iso-propyl                                                                              "        "                                          6-O-1,2:3,4-di-O-iso-                                                          propylidene-D-                                                                 galatopyranose sec.-butyl  "        "                                          6-O-1,2:3,4-di-O-iso-                                                          propylidene-D-                                                                 galatopyranose 3'-butyl    "        "                                          6-O-1,2:3,4-di-O-iso-                                                          propylidene-D-                                                                 galatopyranose 2'-ethyl    H        H                                          6-O-1,2:3,4-di-O-iso-                                                          propylidene-D-                                                                 galatopyranose methyl      H        H                                          ______________________________________                                    

Still other compounds of the general formula S--O--Y, wherein Y is a cyclic monovalent nitrogen-containing organic radical or residue, which may be used in practicing the invention, are as follows:

    ______________________________________                                                      Substituent                                                                    (Y)                                                                                           Substituent                                        Monosaccharide Residue      on the                                             (S)            Cyclic Radical                                                                              Cyclic Radical                                     ______________________________________                                         3-O-1,2-O-isopropylidene-                                                      D-glucofuranose                                                                               4'-piperidyl H                                                  3-O-1,2-O-isopropylidene-                                                      D-glucofuranose                                                                               3'-piperidyl methyl H                                           3-O-1,2-O-isopropylidene-                                                      D-glucofuranose                                                                               2'-piperidyl "                                                  3-O-1,2-O-isopropylidene-                                                      D-glucofuranose                                                                               3'-pyrrolidyl                                                                               "                                                  3-O-1,2-O-isopropylidene-                                                      D-glucofuranose                                                                               2'-pyrrolidyl                                                                               "                                                  6-O-1,2-O-isopropylidene-                                                      D-galatopyranose                                                                              4'-piperidyl H                                                  6-O-1,2-O-isopropylidene-                                                      D-galatopyranose                                                                              3'-piperidyl methyl H                                           6-O-1,2-O-isopropylidene-                                                      D-galatopyranose                                                                              2'-piperidyl "                                                  6-O-1,2-O-isopropylidene-                                                      D-galatopyranose                                                                              3'-pyrrolidyl                                                                               "                                                  6-O-1,2-O-isopropylidene-                                                      D-galatopyranose                                                                              2'-pyrrolidyl                                                                               "                                                  3-O-1,2:5,6-di-O-iso-                                                          propylidene-D-                                                                 glucofuranose  4'-piperidyl H                                                  3-O-1,2:5,6-di-O-iso-                                                          propylidene-D-                                                                 glucofuranose  3'-piperidyl methyl H                                           3-O-1,2:5,6-di-O-iso-                                                          propylidene-D-                                                                 glucofuranose  2'-piperidyl "                                                  3-O-1,2:5,6-di-O-iso-                                                          propylidene-D-                                                                 glucofuranose  3'-pyrrolidyl                                                                               "                                                  3-O-1,2:5,6-di-O-iso-                                                          propylidene-D-                                                                 glucofuranose  2'-pyrrolidyl                                                                               "                                                  6-O-1,2:3,4-di-O-                                                              isopropylidene-D-                                                              galatopyranose 4'-piperidyl H                                                  6-O-1,2:3,4-di-O-                                                              isopropylidene-D-                                                              galatopyranose 3'-piperidyl methyl H                                           6-O-1,2:3,4-di-O-                                                              isopropylidene-D-                                                              galatopyranose 2'-piperidyl "                                                  6-O-1,2:3,4-di-O-                                                              isopropylidene-D-                                                              galatopyranose 3'-pyrrolidyl                                                                               "                                                  6-O-1,2:3,4-di-O-                                                              isopropylidene-D-                                                              galatopyranose 2'-pyrrolidyl                                                                               "                                                  ______________________________________                                    

The present invention also provides certain novel compounds which have wide spectrum antiviral activity. The novel compounds may be defined generically as follows:

3-O-3'-(N',N'-dimethylamino-n-propyl)-1,2-O-isopropylideneglucofuranose,

3-O-4'-(N'-methylpiperidyl)-1,2-O-isopropylideneglucofuranose,

3-O-2'-(N',N'-dimethylaminoethyl)-1,2-O-isopropylideneglucofuranose,

3-O-3'-(2',N',N'-trimethylamino-n-propyl)-1,2-O-isopropylideneglucofuranose

3-O-2'-(N',N'-dimethylaminopropyl)-1,2-O-isopropylideneglucofuranose,

6-O-3'-(N',N'-dimethylamino-n-propyl)-1,2-O-isopropylidenegalactopyranose,

6-O-2'-(N',N'-dimethylaminopropyl)-1,2-O-isopropylidenegalactopyranose,

3-O-3'-(N',N'-dimethylamino-n-propyl)-1,2:5,6-di-O-isopropylideneglucofuranose,

3-O-4'-(N'-methylpiperidyl)-1,2:5,6-di-O-isopropylideneglucofuranose,

3-O-2'-(N',N'-dimethylaminoethyl)-1,2:5,6-di-O-isopropylideneglucofuranose,

3-O-3'-(2',N',N'-trimethylamino-n-propyl)-1,2:5,6-di-O-isopropylideneglucofuranose,

3-O-2'-(N',N'-dimethylaminopropyl)-1,2:5,6-di-O-isopropylideneglucofuranose

6-O-3'-(N',N'-dimethylamino-n-propyl)-1,2:3,4-di-O-isopropylidenegalactopyranose,

6-O-2'-(N',N'-dimethylaminopropyl)-1,2:3,4-di-O-isopropylidenegalactopyranose,

-N',N'-dimethylamino-iso-propyl-2,3:5,6-di-O-isopropylideneglucofuranoside,

and organic and inorganic acid salts thereof.

Species of the foregoing novel compounds which possess striking wide spectrum antiviral activity are as follows:

3-O-3'-(N',N'-dimethylamino-n-propyl)-1,2-O-isopropylidene-D-glucofuranose,

3-O-4'-(N'-methylpiperidyl)-1,2-O-isopropylidene-D-glucofuranose,

3-O-2'-(N',N'-dimethylaminoethyl)-1,2-O-isopropylidene-D-glucofuranose, 3-O-3'-(2',N',N'-trimethylamino-n-propyl)-1,2-O-isopropylidene-D-glucofuranose,

3-O-2'-(N',N'-dimethylaminopropyl)-1,2-O-isopropylidene-D-glucofuranose,

6-O-3'-(N',N'-dimethylamino-n-propyl)-1,2-O-isopropylidene-D-galactopyranose,

6-O-2'-(N',N'-dimethylaminopropyl)-1,2-O-isopropylidene-D-galactopyranose,

3-O-3'-(N',N'-dimethylamino-n-propyl)-1,2:5,6-di-O-isopropylidene-D-glucofuraose,

3-O-4'-(N'-methylpiperidyl)-1,2:5,6-di-O-isopropylidene-D-glucofuranose,

3-O-3'-(2',N',N'-trimethylamino-n-propyl)-1,2:5,6-di-O-isopropylidene-D-glucofuranose,

3-O-2'-(N',N'-dimethylaminoethyl)-1,2:5,6-di-O-isopropylidene-D-glucofuranose,

3-O-2'-(N',N'-dimethylaminopropyl)-1,2:5,6-di-O-isopropylidene-D-glucofuranose,

6-O-3'-(N',N'-dimethylamino-n-propyl)-1,2:3,4-di-O-isopropylidene-D-galactopyranose,

6-O-2'-(N',N'-dimethylaminopropyl)1,2:3,4-di-O-isopropylidene-D-galactopyranose,

α-N',N'-dimethylamino-iso-propyl-2,3:5,6-di-O-isopropylidene-D-glucofuranoside,

and organic and inorganic acid salts thereof.

In general, the preparation of the monosubstituted compounds described herein involves the formation of alkyl ethers or substituted alkyl ethers at selected positions on the desired monosaccharide derivative, such as at position 3-O- of 1,2-O-isopropylidene-D-glucofuranose or 1,2:5,6-di-O-isopropylidene-D-glucofuranose, position 6-O- of 1,2-O-isopropylidene-D-galactopyranose or 1,2:3,4-di-O-isopropylidene-D-galactopyranose, and position 3-O- of 1,2-O-isopropylidene-D-fructopyranose, or 1,2:5,6-di-O-isopropylidene-D-fructopyranose. The condensation of the substituent substrate with the monosaccharide derivative at the desired position may be achieved by various prior art techniques. One method is described in U.S. Pat. No. 2,715,121, issued Aug. 9, 1955, to GLEN et al, the disclosure of which is incorporated herein by reference. The method described in this patent requires extreme reaction conditions and often gives low yields. The product purity is also less than satisfactory.

The preferred method of preparation involves much milder reaction conditions than employed in U.S. Pat. No. 2,715,121. The side reactions are minimized, the purity of the final product is greatly improved and the method may be adapted to a series of solvents having varying properties such as dioxane, tetrahydrofuran and benzene. Briefly, the improved method involves the reaction of a monosaccharide derivative which is blocked with one or more organo groups in the hydroxyl group positions adjacent the desired position to be substituted. The blocked monosaccharide is dissolved in one of the foregoing solvents and is reacted with a halogenated organo amino compound having the desired carbon chain length and configuration in the presence of a base such as sodium hydroxide. Selective removal of one or more blocking groups may be accomplished by hydrolysis under specific conditions resulting in a new product which is to be considered a compound of this invention. The reaction of either the blocked compound or the hydrolyzed compound with any organic or inorganic acid to form a salt thereof or with any organic or inorganic base to form a salt thereof results in a compound of this invention.

It is understood that simple derivatives of the compounds described herein are embraced by the invention. Such derivatives may be prepared by prior art techniques and procedures and used as an ingredient in the therapeutic composition and method of the invention.

For example, the free amine compounds are basic and form organic acid salts and inorganic acid salts, and the resulting salts are useful in the therapeutic composition and method of the invention. The salts may be prepared by the usual prior art techniques, such as by adding the free amine compound to water and then adding the desired organic acid or mineral acid thereto in an amount sufficient to neutralize the free amine. Examples of suitable acids include HCl, HBr, H₂ SO₄, HNO₃, benzoic acid, p-aminobenzoic acid, p-acetamidobenzoic acid, p-hydroxybenzoic acid, alkane sulfonic acid, p-toluene sulfonic acid, acetic acid, alkylcarboxylic acids, oxalic acid, tartaric acid, lactic acid, pyruvic acid, malic acid, succinic acid, gluconic acid and glucuronic acid. The aqueous solution of the resulting salt is evaporated to the volume necessary to assure precipitation of the salt upon cooling. The precipitated salt is recovered by filtration, washed and dried to obtain a final amine salt product. The amine salts are often preferred for use in formulating the therapeutic compositions of the invention as they are crystalline and relatively nonhygroscopic. The amine salts are also better adapted for intramuscular injection than are the free amines.

Prior art blocking techniques may be employed such as acetonization and acetylation. Suitable prior art blocking methods are described in the aforementioned U.S. Pat. No. 2,715,121 and are described in the specific examples appearing hereinafter. In instances where an aldehyde or ketone is reacted with hydroxyl groups on adjacent carbon atoms, the initial compound may be dissolved in the desired aldehyde or ketone under anhydrous conditions and a Lewis acid catalyst is added in a catalytic quantity, such as 1% zinc chloride or anhydrous phosphoric acid. Often acetone is the preferred blocking agent, but aldehydes or ketones of much higher molecular weight may be used when desired such as those containing up to 25 carbon atoms. The reaction mixture is agitated at room temperature for a prolonged reaction period, such as 24-48 hours. The compound may be blocked in a plurality of positions, such as the 1,2- and 5,6- positions. It is usually preferred to block positions such as the 1,2- positions as the resulting partially blocked compound is much less toxic than compounds blocked in all available hydroxyl groups.

It is also possible to block one or more free hydroxyl positions of the compound with an ester group, wherein the carboxylic acid residue contains 1-18 and preferably 1-3 carbon atoms. The ester derivatives likewise may be prepared following prior art techniques such as by reacting a carboxylic acid anhydride with the compound following prior art practices. Additionally, the α or β alkyl derivatives of monosaccharide derivatives such as 2,3:5,6-di-O-isopropylidene-D-glucofuranoside may be prepared following prior art techniques. In this latter instance, the compound is dissolved in a dry alcohol having the desired carbon chain length with aforementiond residua and reacted with the compound in the presence of a catalyst such as hydrogen chloride of Dowex 50 H+ resin. While the above discussed derivatives are presently preferred, it is understood that still other simple derivatives may be prepared following prior art techniques and then used in practicing the present invention. In addition to the foregoing, the compounds may also include monosubstitutions of monosaccharide derivatives in which the substrate ##STR5## may be replaced by a substituent R₇, where R₇ is a deoxymonosaccharide derivative of halogen, keto, amino, lower alkyl, mercapto, alkenyl, alkynyl, aromatic, heterocyclic or alkylcarboxylic acid and its derivatives. R₇ may also represent the same groups as the above substrate of the monosaccharide derivative ethers. Still other antiviral agents have a general formula S--O--Y wherein Y is --R₈ --S--R₉, where R₈ is a saturated or unsaturated hydrocarbon radical containing 1-7 carbon atoms and R₉ is a monovalent saturated or unsaturated hydrocarbon radical containing 1-7 carbon atoms and hydrogen.

The compounds of the invention are especially useful as wide spectrum antiviral agents for the therapeutic treatment of warm-blooded animals. They exhibit potent antiviral activity against both RNA and DNA viruses, contrary to the prior art antiviral agents. The compounds of the present invention exhibit marked suppression of virus particle multiplication and virus-induced cell injury in animal and human cell tissue culture systems against such widely varying viruses as herpes simplex, influenza A, mumps, poliovirus and rhinovirus. In tests in the whole animal, the compounds can reduce mortality and morbidity manifestations of influenza A infection by from 50% to 85%.

The compounds of the present invention may be administered to human patient or animal to be treated either orally or by parenteral administration. When the therapeutic composition is to be administered orally, the compound may be admixed with a prior art filler and/or binder such as starch and a disintegrator, and the admixture is pressed into a tablet of a size convenient for oral administration. Capsules also may be filled with the powdered therapeutic composition and administered orally. Alternatively, a water solution or suspension of the therapeutic composition may be admixed with a flavored syrup such as cherry syrup and administered orally. When the therapeutic composition is administered by intramuscular injection, the compound is usually dissolved in a physiological saline solution which contains sodium chloride in sufficient concentration to make the overall solution to be injected isotonic to body fluids. A salt of the free amine compound is usually preferred in instances where the compound is administered by intramuscular injection. In treating upper respiratory viral infections, the salt form in aqueous solution may also be administered by nasopharyngeal spray. Administration also may be by means of a suppository in patients unable to retain medication administered by mouth.

The dosage may be varied over extremely wide limits, as the compounds are effective at low dosage levels and are relatively free of toxicity and adverse side effects. The compounds may be administered in the minimum quantity which is therapeutically effective, and the dosage may be increased as desired up to the maximum dosage tolerated by the patient. Animal toxicity data indicate that the limiting nontoxic dosage may be up to 100-200 times the minimum effective dosage. Also, it is not necessary to carefully control the dosage for patients sensitive to the prior art antiviral drugs. As a general rule, the compound may be administered in an amount of about 1-40 milligrams per kilogram of body weight per day, and preferably in an amount of about 2-20 miligrams per kilogram per day, over the period required for treatment of the viral infection.

Surprisingly, the compounds described herein have still other unusual and unexpected therapeutically valuable properties. The learning of new tasks is enhanced. The therapeutic composition also protects against death due to water deprivation. The buffer capacity of the compounds over a pH range of approximately 7-9.8 is very good and they may be used for this purpose. Certain compounds also exhibit lubricative properties and may be used as a specialized lubricant. Compounds such as 3-O-D-glucopropionitrile and its derivatives are photosensitive and may be used in photographic applications.

It has been further discovered that the normal life span of tissue culture cells being grown in a prior art tissue culture medium may be extended very substantially and often by several fold by growing the cells in a tissue culture medium which contains an effective amount of one or more of the antiviral compounds described herein. This variant of the present invention is especially useful in the growing of human embryo cells and it has been observed that such cells survive for a significantly longer period of time in a tissue culture medium in the presence of as little as 2 micrograms per milliliter of one or more of the antiviral compounds described herein. However, much larger quantities of the compound may be present, such as the quantity described herein in the treatment of tissue culture cells infected with a virus, or in amounts up to the tolerance level of the cells. Preferably, the compound is 3-O-3'(N',N'-dimethylamino-n-propyl)-1',2-O-isopropylidene glucofuranose. This variant of the invention reduces research costs due to the longer life span of the tissue culture cells. It also has other positive effects as the surviving cells tend to be more vigorous and in a better state of preservation and more consistent research results are obtained.

It has also been discovered that the antiviral compounds disclosed herein, the pharmaceutical compositions containing the same, and the method of the invention are effective in the treatment of metastatic cancer in mice. In practicing this variant of the invention, a mouse having a metastatic cancer, such as carcinoma, is treated by administering thereto a therapeutically effective amount of at least one antiviral compound disclosed herein. The compound may be administered at the dosage level described herein for common viral infections such as influenza. Often much larger quantities are more effective such as 10-50 times this amount, or quantities within the tolerance level of the mouse regardless of the amount. Death from cancer is caused by metastatic spread of the tumor cells, which in turn results from a greater freedom to translocate that individual cells develop when they become cancerous (Leighton, J., The Spread of Cancer. Academic Press, New York and London, 1967). The compounds used in the treatment of cancers specifically prevent this tendency to metastasis, thereby rendering the cancer non-malignant and allowing the mouse to live.

The compounds used in the aforementioned treatment of metastatic cancer and/or in the tissue culture medium in the growing of tissue culture cells are preferably the antiviral compounds disclosed herein. However, it is understood that the antiviral compounds disclosed in my earlier filed application Ser. No. 337,134 also are useful for this purpose and may be substituted in equal quantities. The teachings of application Ser. No. 337,134 are therefore incorporated herein by reference.

The following specific examples further illustrate the present invention.

EXAMPLE 1

To a solution of 104 g (0.4 mole) of 1,2:5,6-di-O-isopropylidene-D-glucofuranose in 550 ml of 1,4-dioxane was added 189.7 g (1.2 mole) of 3-chloro-N,N-dimethylamino propane in the form of the hydrochloride salt and 144 g (3.6 mole) of sodium hydroxide. The suspension was mechanically stirred and heated to reflux for 18 hours. The reaction mixture thus prepared was filtered, the solids were washed with 1,4-dioxane and the washings were combined with the filtered liquid. The solvent was removed under reduced pressure and an amber-colored viscous oil was obtained.

The oil was distilled under high vacuum (less than 1 mm Hg) while using a very slight dry nitrogen purge to obtain high and low boiling fractions. The low boiling fraction was identified as unreacted 3-chloro-N,N-dimethylamino propane. The high boiling fraction had a boiling point of 148°-154° C. at 2.5 mm Hg and was a clear viscous oil with an optical rotation of {α}_(D) ²⁵ =-19.3° neat (100 mm) and a density of 0.95 g/cc. The refractive index was η_(D) ²⁶ =1.4576. Gas chromatography showed a purity greater than 99%. An elemental analysis showed: C, 59.13; H, 8.99; N, 4.12; O, 27.7. The yield was 80% of the novel compound 1,2:5,6-di-O-isopropylidene-3-O-3'-(N',N'-dimethylamino-n-propyl)-D-glucofuranose.

A portion of the above oil (10 g) was hydrolyzed in aqueous sulfuric acid at a pH value of 1.9-2.1 for 10 hours with refluxing. The resulting solution was adjusted to a pH value of 4.5 with saturated Ba(OH)₂ solution centrifuged, and filtered through an ultrafine filter. The filtrate was lyophillized to a white-to-slightly yellow solid having a melting point of 78°-80° C. Gas chromatography data indicated above 99% purity of the novel compound 3-O-3'-(N',N'-dimethylamino-n-propyl)-D-glucopyranose. In thin-layer chromatography, the flow rate on silica gel with a solvent mixture composed of n-propanol, ethyl acetate, H₂ O and NH₃ in the ratio by volume of 60:10:30:10, respectively, was R_(f) =0.356.

A portion of the oil is partially dehydrolyzed to 1,2-O-isopropylidene-3-O-3'-(N',N'-dimethylamino-n-propyl)-D-glucofuranose by dissolving it in distilled water and adjusting the pH of the approximately 1 M solution to 3.0±0.2 with 6N HCl. The solution is extracted twice with chloroform and the clear aqueous solution is refluxed for about 2 hours. Completion of partial hydrolysis reaction was monitored by gas chromatography from disappearance of the peak of parent compound and appearance of a new peak with larger retention time. The solution is then cooled, made alkaline with 30% sodium hydroxide to pH 10.5 and then extracted with chloroform. The chloroform phase is separated, dried over anhydrous magnesium sulfate and vacuum distilled to remove the solvent. The resulting colorless viscous oil has optical rotation of α_(neat) °=-12° and refractive index of 1.4687 at 25° C. Alternatively, the compound can be obtained as the hydrochloride salt by lyophillizing the aqueous solution after partial hydrolysis at pH 4.0-4.5. A white crystalline material is obtained which is recrystallized from methanol. The crystalline hydrochloride of 1,2-O-isopropylidene-3-O-3'-(N',N'-dimethylamino-n-propyl)-D-glucofuranose has a melting point of 181°-183° C. and purity as indicated by gas chromatography is 98+%. Infrared spectrophotometry indicates the presence of a strong --OH band which is not present in the parent oil. The elemental analysis for the hydrochloride salt in a typical batch showed: C, 49.09; H, 8.40; N, 4.14; Cl, 10.32; O, 28.12. Theoretical values are as follows: C, 49.19; H, 8.19; N, 4.09; Cl, 10.39; O, 28.11.

The gas-liquid chromatograms for the above intermediate and final novel compounds were run on a Beckman GC, Model 72-5 with a hydrogen flame detector. The column used for the intermediate novel compound was a commercially available SE-52 column, wherein methyl phenyl resins act as stationary phases supported on Chromosorb W (H.P.) which is made by Johns-Manville Corporation. The final novel compound was chromatographed on a Chromosorb 103 glass column, which is packed with porous resins. The foregoing materials are commercially available.

EXAMPLE 2

Starting with 51 g (0.3 mole) of 4-chloro-N-methylpiperidine hydrochloride and 26 g (0.1 mole) of 1,2:5,6-di-O-isopropylidene-D-glucofuranose and 36 g of NaOH in 150 ml 1,4-dioxane, condensation was accomplished using the general procedure outlined in Example 1. The residue remaining following vacuum distillation was dissolved and recrystallized from hot methanol. The melting point was 106°-107.5° C. (sharp).

Hydrolysis of the above product in H₂ SO₄ at a pH value of 2.1 yielded 3-O-4'-(N'-methylpiperidyl)-D-glucopyranose having an optical rotation of {α}_(D) ²⁵ =+38.42° in H₂ O. A gas chromatography analysis in accordance with Example 1 indicated that the purity of the product was in excess of 96%. The melting point was 62°-65° C.

EXAMPLE 3

A solution of 0.1 mole of 1,2:5,6-di-O-isopropylidene-D-glucofuranose in 50 ml of tetrahydrofuran was added to a suspension of 0.3 mole of 2-chloro-N,N-diethylaminoethane hydrochloride and 36 g of sodium hydroxide in 100 ml of tetrahydrofuran. The suspension was mechanically stirred and refluxed overnight and the reaction mixture was treated as set out in Example 1. The desired product, 1,2:5,6-di-O-isopropylidene-3-O-2'-(N',N'-diethylaminoethyl)-D-glucofuranose was obtained as a clear yellow liquid (boiling point 144°-150° C./0.15 mm Hg) having an optical rotation of {α}_(D) ²⁸ =-20.6° neat and a refractive index of η_(D) ²⁵ =1.4532. The liquid solidified on exposure to air, probably due to formation of the carbonate salt. The yield was 85%. Ten grams of the above product were hydrolyzed with aqueous sulfuric acid at a pH value of 1.9-2.1 for 10 hours under reflux. The resulting solution was adjusted to a pH value of 4-5 with saturated barium hydroxide solution and then centrifuged and filtered. Lyophillization of the filtrate yielded 6.55 g of light brown crystalline 3-O-2'-(N',N'-diethylaminoethyl)-D-glucopyranose. The optical rotation in water was {α}_(D) ²⁵ =+36.30°. A gas chromatography analysis in accordance with Example 1 indicated that the purity was in excess of 99%.

EXAMPLE 4

To 26 g (0.1 mole) of 1,2:5,6-di-O-isopropylidene-D-glucofuranose and 36 g (0.9 mole) of sodium hydroxide in 150 ml of refluxing tetrahydrofuran was added dropwise over 1 hour 0.3 mole of 3-bromopropionitrile in 50 ml of tetrahydrofuran. The reaction mixture was refluxed for an additional 6 hours and then filtered. The solids were washed with tetrahydrofuran and the washings were combined with the filtrate. The solvent was removed under reduced pressure and solid 1,2:5,6-di-O-isopropylidene-3-O-3'-propionitrile-D-glucofuranose was obtained. The decomposition point was 165° C. and it was light sensitive indicating utility in photographic applications.

Five grams (0.016 mole) of the above product was dissolved in anhydrous ether and added dropwise to a suspension of 0.76 g (0.02 mole) of lithium aluminum hydride in ether. The resulting complex was dissolved in cold hydrochloric acid and neutralized rapidly with sodium bicarbonate. The suspension thus produced was extracted with chloroform and the solvent was removed to obtain a yellow oil in a yield of 250 mg. Gas chromatography in accordance with Example 1 indicated a purity of 98% and there was a sharp infrared band at 3400 cm⁻¹. The oil was hydrolyzed at a pH value of 2.1 in sulfuric acid and lyophillized to dryness. The yield was 85 mg of 3-O-3'-(n-propylamino)-D-glucopyranose.

EXAMPLE 5

The 3-O-2'-(N',N'-dimethylaminopropyl) derivative of 1,2:5,6-di-O-isopropylidene-D-glucofuranose was prepared by condensing 0.1 mole of 1,2:5,6di-O-isopropylidene-D-glucofuranose with 0.3 mole of 2-chloro-N,N-dimethylamino propane hydrochloride in the presence of 0.9 mole of sodium hydroxide in 150 ml of 1,4-dioxane. The reaction mixture was fractionally distilled under reduced pressure to obtain a yellow viscous oil (boiling point 142°-145° C./0.07 mm Hg) in 81% yield. The optical rotation was {α}_(D) ²⁵ =-21.5° neat and the refractive index was η_(D) ²⁵ =1.4549. Gas chromatography in accordance with Example 1 indicated only one component.

The above prepared yellow viscous oil (10 g) was hydrolyzed with aqueous sulfuric acid at a pH value of 2.0 by refluxing for 10 hours. The pH value of the hydrolysate was adjusted to 4-5 with saturated barium hydroxide solution, filtered and lyophillized to obtain 10.5 g of light yellow crystals of 3-O-2'-(N',N'-dimethylaminopropyl)-D-glucopyranose. The optical rotation in water was {α}_(D) ²⁵ =+37.86°. Gas chromatography in accordance with Example 1 indicated a purity in excess of 82%.

A portion of the oil, 1,2:5,6-di-O-isopropylidene-3-O-2'-(N',N'-dimethylaminopropyl)-D-glucofuranose, is partially hydrolyzed at pH 3.0±0.2 as indicated in Example 1. A white crystalline hydrochloride salt is obtained on lyophillization. The salt obtained is highly hygroscopic, with gas chromatographic purity being of the order of 80%.

EXAMPLE 6

To 0.1 mole of 1,2:5,6-di-O-isopropylidene-D-glucofuranose was added 0.3 mole of 2,N,N-trimethylaminopropyl chloride hydrochloride along with 36 g of sodium hydroxide. The general reaction procedure was in accordance with Example 1. The oil resulting from the reaction had a boiling point of 144°-146° C. at 0.6 mm Hg and an optical rotation of {α}_(D) ²⁰ =-20.05° neat.

The above product was hydrolyzed according to the general method outlined in Example 1 to obtain the desired 3-O-3'-(2',N',N'-trimethylamino-n-propyl)-D-glucopyranose. The optical rotation of the product in water was {α}_(D) ²⁰ =+38.0°.

A portion of the oil, 1,2:5,6-di-O-isopropylidene-3-O-3'-(2',N',N'-trimethylamino-n-propyl)-D-glucofuranose, is partially hydrolyzed at pH 3.0±0.2 according to the procedure mentioned in Example 1. A white crystalline 1,2-O-isopropylidene-3-O-3'-(2',N',N'-trimethylamino-n-propyl)-D-glucofuranose hydrochloride was obtained which is highly hygroscopic in nature. Optical rotation of the hydrochloride salt at pH 7.0 and 25° C. is -21.33°. Gas chromatography analysis indicated better than 99% pure major component.

EXAMPLE 7

Using the general method outlined in Example 1, 0.02 mole of 1,2:5,6-di-O-isopropylidene-D-glucofuranose in 1,4-dioxane was reacted with 0.0225 mole of 2-(2-chloroethyl)-N-methylpyrrolidine hydrochloride and 0.0675 mole of sodium hydroxide. After 18 hours, the solvent was removed and the resulting orange oil was vacuum distilled under nitrogen. The residue consisted of the desired product, 1,2:5,6-di-O-isopropylidene-3-O-2'-{2'-(N"-methyl)-pyrrolidyl}-ethyl-D-glucofuranose having an optical rotation of {α}_(D) ²⁵ =-22.95° in chloroform.

EXAMPLE 8

1,2:5,6-di-O-isopropylidene-D-glucofuranose (0.1 mole) and N-(2-chloroethyl)-pyrrolidine hydrochloride (0.15 mole) are mechanically stirred and refluxed with 0.45 mole of sodium hydroxide in 150 ml of tetrahydrofuran for 18 hours. The tetrahydrofuran is removed from the reaction products and the resulting oil is vacuum distilled under nitrogen. The 3-O-2'-{N'-pyrrolidyl)-ethyl}-1,2:5,6-di-O-isopropylidene-D-glucofuranose derivative has a boiling point of 165°-171° C./0.15 mm Hg. Gas chromatography indicates a purity of 99%. Using the hydrolysis procedure outlined in Example 1, 10 g of the blocked oil was hydrolyzed and lyophillized giving a white hygroscopic crystalline solid.

EXAMPLE 9

The N',N'-dimethylamino-n-pentyl derivative of 1,2:5,6-di-O-isopropylidene-D-glucofuranose is made by condensing N,N-dimethylamino-n-pentyl-5-chloride hydrochloride with 1,2:5,6-di-O-isopropylidene-D-isopropylidene-D-glucofuranose in the presence of pulverized sodium hydroxide in freshly purified, dry 1,4-dioxane as described in the procedure in Example 1. The product was confirmed by gas chromatography and infrared spectra.

N,N-dimethylamino-n-pentyl chloride hydrochloride is made from a commercially available sample of N,N-dimethylamino-n-pentyl alcohol by treatment with thionyl chloride (SOCl₂). Specifically, 10.7 g of thionyl chloride in a 250 ml three neck round bottom flask is cooled in a salt-ice water bath and stirred vigorously. To the cooled solution is added, dropwise, 10 g of N,N-dimethylamino-n-pentyl alcohol. The reaction is exothermic and the temperature is carefully controlled. The mixture is stirred for 1 hour after the evolution of SO₂ and HCl subsides. The mixture is brought to room temperature and allowed to stir overnight. Absolute alcohol is added to destroy excess thionyl chloride. Ten grams of crude N,N-dimethylamino-n-pentyl chloride hydrochloride is obtained as a white solid. This is used directly for the condensation reaction with 1,2:5,6-di-O-isopropylidene-D-glucofuranose without further purification. The alcohol and chloride can be resolved on a Chromosorb 103 gas chromatography column.

EXAMPLE 10

Bromine (9.8 g) was added slowly and dropwise to a mechanically stirred mixture of 50 g of cracked ice and a chilled aqueous sodium hydroxide solution (7 g/20 ml water). After the addition of bromine is complete, 15 g of 1,2:5,6-di-O-isopropylidene-3-O-acetamido-D-glucofuranose (prepared by the general procedure outlined in Example 1 by the condensation of 1,2:5,6-di-O-isopropylidene-D-glucofuranose with 2-chloroacetamide in the presence of sodium hydroxide) is added in four portions 15 minutes apart. The reaction mixture is heated for 1 hour in a water bath. After this time, an additional portion of the aqueous solution of sodium hydroxide (20 g/20 ml) is added and heating is continued for another hour. The mixture is cooled and extracted three times with ether. The ether extract is dried over anhydrous magnesium sulfate. The yellow hygroscopic solid remaining after evaporating off the ether is the desired 1,2:5,6-di-O-isopropylidene-3-O-aminomethyl-D-glucofuranose derivative. The product was identified by the disappearance of the carbonyl stretching at 1670 cm⁻¹ found in the parent acetamido compound.

EXAMPLE 11

Well established methodology of the prior art was employed to determine the antiviral potency of derivatives of 1,2-O-isopropylidene-D-glucofuranose. HCl against poliovirus, type 1, and rhinovirus, type 1A, in tissue cultures at 37° C., employing HeLa cells with an agar overlay and WI-38 cells respectively. (See Wallis, C., F. Morales, J. Powell, and J. L. Melnick, Plaque enhancement of enteroviruses by magnesium chloride, cysteine, and pancreatin. J. Bacteriol. 91:1932-1935, 1966.) Poliovirus cell injury was determined by the study of plaque formation and rhinovirus was examined for cytopathic effect. In Table I, the virus inhibiting effects of three concentrations of the 3-O-3'-(N',N'-dimethylamino-n-propyl) derivative are depicted. The results are given as the degree of inhibition of infectivity, identified as plaque formation in the poliovirus system and as cytopathic effect in the system studying rhinovirus. The results indicate that, at the appropriate dose, the drug can completely inhibit 1,000 plaque forming units (PFU) of poliovirus and a 1,000 TCID₅₀ dose of rhinovirus 1A, which is a virus dose 1,000 times that amount required to kill 50% of the tissue cultured cells.

                                      TABLE I                                      __________________________________________________________________________     DERIVATIVES OF 1,2-O-ISOPROPYLIDENE-D-GLUCOFURANOSE HCL                        SUMMARY OF ANTIVIRAL ACTIONS IN TISSUE CULTURE                                                     Virus                                                      Derivative                                                                             Dose System Type  Titer  Determination                                                                          Drug Effect                           __________________________________________________________________________     3-O-3'-(N',N'-                                                                          1 μg/ml                                                                         HeLa cells in                                                                         Poliovirus                                                                            50 PFU.sup.1                                                                         Plaque number                                                                          Total inhibition                      dimethylamino-                                                                              vitro with                                                                            type 1                                                     n-propyl)    agar overlay                                                      3-O-3'-(N',N'-                                                                         20 μg/ml                                                                         HeLa cells in                                                                         Poliovirus                                                                            250 PFU                                                                              "       "                                     dimethylamino-                                                                              vitro with                                                                            type 1                                                     n-propyl)    agar overlay                                                      3-O-3'-(N',N'-                                                                         40 μg/ml                                                                         HeLa cells in                                                                         Poliovirus                                                                           1000 PFU                                                                              "       "                                     dimethylamino-                                                                              vitro with                                                                            type 1                                                     n-propyl)    agar overlay                                                      3-O-3'-(N',N'-                                                                          2 μg/ml                                                                         WI-38 cells                                                                           Rhinovirus                                                                            100 TCID.sub.50.sup.2                                                                Cytopathic                                                                             "                                     dimethylamino-      type 1A      effect                                        n-propyl)                                                                      3-O-3'-(N',N'-                                                                         20 μg/ml                                                                         "      Rhinovirus                                                                           1000 TCID.sub.50                                                                      Cytopathic                                                                             "                                     dimethylamino-      type 1A      effect                                        n-propyl)                                                                      3-O-3'-(N',N'-                                                                         40 μg/ml                                                                         "      Rhinovirus                                                                           1000 TCID.sub.50                                                                      Cytopathic                                                                             "                                     dimethylamino-      type 1A      effect                                        n-propyl)                                                                      __________________________________________________________________________      .sup.1 plaque forming units.                                                   .sup.2 tissue culture infectious dose involving 50% of cells.            

EXAMPLE 12

Derivatives of 1,2-O-isopropylidene-D-glucofuranose hydrochloride were examined for their capacity to suppress influenza A2 disease in mice and for their capacity to suppress death and nonlethal nervous system disease produced by the encephalomyocarditis virus in mice. In these studies, drug effect on lung pathology produced by a 15 ID₅₀ dose of influenza virus was examined. This dose is 15 times the dose that produces disease in 50% of the animals. Disease and drug effect on disease were determined by lung weight increase and reduction thereof. In the encephalomyocarditis study, 10 times the dose capable of killing 50% of the animals was given, and the degree of nonlethal disease and death were determined, as well as drug inhibition of both of these parameters. The results for these experiments are summarized in Table II, and indicate the production of significant reduction in lung weight increase by drug, as well as a significant inhibition of death and nonlethal disease produced by encephalomyocarditis virus. These effects were more potent for the 3-O-3'-(N',N'-dimethylamino-n-propyl) derivative than for the other two derivatives studied.

                                      TABLE II                                     __________________________________________________________________________     DERIVATIVES OF 1,2-O-ISOPROPYLIDENE-D-GLUCOFURANOSE HCL                        SUMMARY OF ANTIVIRAL ACTIONS IN VIVO IN MICE                                                         Virus                                                    Derivative                                                                             Dose  System  Type  Titer                                                                               Determination                                                                         Drug Effect                            __________________________________________________________________________     3-O-3'-(N',N'-                                                                          20 mg/Kg                                                                            Mouse in vivo                                                                          Influenza                                                                            15 ID.sub.50.sup.1                                                                  Lung weight                                                                           Significant re-                        dimethylamino-        type A     increase                                                                              duction in lung                        n-propyl)                               weight increase                        3-O-3'-(N',N'-                                                                          80 mg/Kg                                                                            Mouse in vivo                                                                          Encephalo-                                                                           10 LD.sub.50.sup.2                                                                  Involvement                                                                           Significant in-                        dimethylamino-        myocarditis                                                                               of CNS.sup.3 and                                                                      hibition of death                      n-propyl)                        death  and nonlethal                                                                  disease                                3-O-3'-(N',N'-                                                                         160 mg/kg                                                                            "       Encephalo-                                                                           "    Involvement                                                                           Significant in-                        dimethylamino-        myocarditis                                                                               of CNS.sup.3 and                                                                      hibition of death                      n-propyl)                        death  and nonlethal                                                                  disease                                3-O-2'-(N',N'-                                                                          80 mg/Kg                                                                            "       Encephalo-                                                                           "    Involvement                                                                           Inhibition sig-                        dimethylamino-        myocarditis                                                                               of CNS.sup.3 and                                                                      nificant, but less                     iso-propyl)                      death  than n-propyl                                                                  derivative                             3-O-2'-(N',N'-                                                                         160 mg/kg                                                                            "       Encephalo-                                                                           "    Involvement                                                                           Inhibition sig-                        dimethylamino-        myocarditis                                                                               of CNS.sup.3 and                                                                      nificant, but less                     iso-propyl)                      death  than n-propyl                                                                  derivative                             3-O-3'-(2',N',                                                                          80 mg/Kg                                                                            "       Encephalo-                                                                           "    Involvement                                                                           Inhibition sig-                        N'-trimethyl-         myocarditis                                                                               of CNS.sup.3 and                                                                      nificant, but less                     amino-n-propyl)                  death  than n-propyl                                                                  derivative                             3-O-3'-(2',N',                                                                         160 mg/Kg                                                                            "       Encephalo-                                                                           "    Involvement                                                                           Inhibition sig-                        N'-trimethyl-         myocarditis                                                                               of CNS.sup.3 and                                                                      nificant, but less                     amino-n-propyl)                  death  than n-propyl                                                                  derivative                             __________________________________________________________________________      .sup.1 infectious dose involving 50% of animals.                               .sup.2 lethal dose killing 50% of animals.                                     .sup.3 central nervous system.                                           

EXAMPLE 13

Human embryonic fibroblast cells, WI-38 type, were obtained from Microbiological Associates and grown in maintenance medium 199 with 1% fetal calf serum in the presence and absence of either 2, 20, or 40 μg/ml of 1,2-O-isopropylidene-3-O-3'-(N',N'-dimethylamino-n-propyl)-D-glucofuranose. HCl at 37° C. and 34° C. For cells grown at 37° C., survival of tissue cultured cells in the absence of drug diminished progressively through day 15, at which time 95% of cells failed to metabolize and no longer formed a monolayer. At 34° C., by 72 hours 95% of cells without drug were no longer actively metabolizing as determined by pH and a monolayer was no longer evident under microscopic examination. Addition of drug in the concentrations described above reduced this loss of viability by 75% at 15 days and 72 hours at 37° C. and 34° C. respectively.

EXAMPLE 14

C57B1/6J mice bearing transplanted melanoma B-16 were obtained from The Jackson Laboratories. This tumor was transplanted into recipient C57BL/6J mice at 10 days and the behavior of tumor growth in recipient mice was observed over 2 months. During this period, 90% of control animals died manifesting metastatic spread to the liver, bowel and kidney. Animals treated with 80 mg/Kg per day 1,2-O-isopropylidene-3-O-3"-(N',N'-dimethylamino-n-propyl)-D-glucofuranose. HCl, injected subcutaneously, exhibited significant central necrosis of primary tumors and only 15% succumbed to such cancer metastasis. 

I claim:
 1. A compound selected from the group consisting of3-O-3'-(N',N'-dimethylamino-n-propyl)-1,2-O-isopropylideneglucofuranose, 3-O-4'-(N'-methylpiperidyl)-1,2-O-isopropylidenglucosefuranose, 3-O-2'-(N',N'-dimethylaminoethyl)-1,2-O-isopropylideneglucofuranose, 3-O-3'-(2',N',N'-trimethylamino-n-propyl)-1,2-O-isopropylideneglucofuranose 3-O-2'-(N',N'-dimethylaminopropy)-1,2-O-isopropylideneglucosefuranose, 6-O-3'-(N',N'-dimethylamino-n-propyl)-1,2-O-isopropylidenegalactopyranose, 6-O-2'-(N',N'-dimethylaminopropyl)-1,2-O-isopropylidenegalactopyranose, 3-O-3'-(N',N'-dimethylamino-n-propyl)-1,2:5,6-di-O-isopropylideneglucofuranose, 3-O-4'-(N'-methylpiperidyl)-1,2:5,6-di-O-isopropylideneglucofuranose, 3-O-2'-(N',N'-dimethylaminoethyl)-1,2:5,6-di-O-isopropylideneglucofuranose, 3-O-3'-(2',N',N'-trimethylamino-n-propyl)-1,2:5,6-di-O-isopropylideneglucofuranose, 3-O-2'-(N',N'-dimethylaminopropyl)-1,2:5,6-di-O-isopropyleneglucofuranose, 6-O-3'-(N',N'-dimethylamino-n-propyl)-1,2:3,4-di-O-isopropylidenegalactopyranose, 6-O-2'-(N',N'-dimethylaminopropyl)-1,2:3,4-di-O-isopropylidenegalactopyranose, α-N',N'-dimethylamino-iso-propyl-2,3:5,6-di-O-isopropylideneglucofuranoside,and therapeutically effective and acceptable organic and inorganic acid salts thereof.
 2. A compound selected from the group consisting of3-O-3'-(N',N'-dimethylamino-n-propyl)-1,2-O-isopropylidene-D-glucofuranose, 3-O-4-(N'-methylpiperidyl)-1,2-O-isopropylidene-D-glucofuranose, 3-O-2'-(N',N'-dimethylaminoethyl)-1,2-O-isopropylidene-D-glucofuranose, 3-O-3'-(2',N',N'-trimethylamino-n-propyl)-1,2-O-isopropylidene-D-glucofuranose, 3-O-2'-(N',N'-dimethylaminopropyl)-1,2-O-isopropylidene-D-glucofuranose, 6-O-3'-(N',N'-dimethylamino-n-propyl)-1,2-O-isopropylidene-D-galactopyranose, 6-O-2'-(N',N'-dimethylaminopropyl)-1,2-O-isopropylidene-D-galactopyranose, 3-O-3'-(N',N'-dimethylamino-n-propyl)-1,2:5,6-di-O-isopropylidene-D-glucofuranose, 3-O-4'-(N'-methylpiperidyl)-1,2:5,6-di-O-isopropylidene-D-glucofuranose, 3-O-2'-(N',N'-dimethylaminoethyl)-1,2:5,6-di-O-isopropylidene-D-glucofuranose, 3-O-3'-(2',N',N'-trimethylamino-n-propyl)-1,2:5,6-di-O-isopropylidene-D-glucofuranose, 3-O-2'-(N',N'-dimethylaminopropyl)-1,2:5,6-di-O-isopropylidene-D-glucofuranose, 6-O-3'-(N',N'-dimethylamino-n-propyl)-1,2:3,4-di-O-isopropylidene-D-galactopyranose, p1 6-O-2'-(N',N'-dimethylaminopropyl)-1,2:3,4-di-O-isopropylidene-D-galactopyranose, α-N',N'-dimethylamino-iso-propyl-2,3:5,6-di-O-isopropylidene-D-glucofuranoside,and therapeutically effective and acceptable organic and inorganic acid salts thereof.
 3. A compound in accordance with claim 2 wherein the compound is 3-O-3'-(N',N'-dimethylamino-n-propyl)-1,2-O-isopropylidene-D-glucofuranose
 4. A compound in accordance with claim 2 wherein the compound is3-O-4'-(N'-methylpiperidyl)-1,2-O-isopropylidene-D-glucofuranose.
 5. A compound in accordance with claim 2 wherein the compound is3-O-2'-(N',N'-dimethylaminoethyl)-1,2-O-isopropylidene-D-glucofuranose.
 6. A compound in accordance with claim 2 wherein the compound is3-O-3'-(2',N',N'-trimethylamino-n-propyl)-1,2-O-isopropylidene-D-gulcofuranose.
 7. A compound in accordance with claim 2 wherein the compound is3-O-2'-(N',N'-dimethylaminopropyl)-1,2-O-isopropylidene-D-glucofuranose.
 8. A compound in accordance with claim 2 wherein the compound is6-O-3'-(N',N'-dimethylamino-n-propyl)-1,2-O-isopropylidene-D-galactopyranose.
 9. A compound in accordance with claim 2 wherein the compound is6-O-2'-(N',N'-dimethylaminopropyl)-1,2-O-isopropylidene-D-galactopyranose.
 10. A compound in accordance with claim 2 wherein the compound is3-O-3'-(N',N'-dimethylamino-n-propyl)-1,2:5,6-di-O-isopropylidene-D-glucofuranose.
 11. A compound in accordance with claim 2 wherein the compound is3-O-4'-(N'-methylpiperidyl)-1,2:5,6-di-O-isopropylidene-D-gulcofuranose.
 12. A compound in accordance with claim 2 wherein the compound is3-O-2'-(N',N'-dimethylaminoethyl)-1,2:5,6-di-O-isopropylidene-D-glucofuranose.
 13. A compound in accordance with claim 2 wherein the compound is3-O-3'-(2',N'N'-trimethylamino-n-propyl)-1,2:5,6-di-O-isopropylidene-D-glucofuranose.
 14. A compound in accordance with claim 2 wherein the compound is3-O-2'-(N',N'-dimethylaminopropyl)-1,2:5,6-di-O-isopropylidene-D-glucofuranose.
 15. A compound in accordance with claim 2 wherein the compound is6-O-3'-(N',N'-dimethylamino-n-propyl)-1,2:3,4-di-O-isopropylidene-D-galactopyranose.
 16. A compound in accordance with claim 2 wherein the compound is6-O-2'-(N',N'-dimethylaminopropyl)-1,2:3,4-di-O-iospropylidene-D-galactopyranose.
 17. A compound in accordance with claim 2 wherein the compound isα-N',N'-dimethylamino-iso-propyl-2,3:5,6-O-isopropylidene-D-glucofuranoside.
 18. A compound in accordance with claim 1 wherein the compound is in the form of a salt of an acid selected from the group consisting of HCl, HBr, H₂ SO₄, HNO₃, benzoic acid, p-aminobenzoic acid, p-acetamidobenzoic acid, p-hydroxybenzoic acid, alkane sulfonic acids, p-toluene sulfonic acid, lower alkyl monocarboxylic acids, oxalic acid, tartaric acid, lactic acid, pyruvic acid, malic acid, succinic acid, gluconic acid and glucuronic acid.
 19. A compound in accordance with claim 18 wherein the said compound is 3-O-3'-(N',N'-dimethylamino-n-propyl)-1,2-O-isopropylideneglucofuranose.
 20. A compound in accordance with claim 19 wherein the said acid is HCl.
 21. A compound in accordance with claim 2 wherein the compound is in the form of a salt of an acid selected from the group consisting of HCl, HBr, H₂ SO₄, HNO₃, benzoic acid, p-aminobenzoic acid, p-acetamidobenzoic acid, p-hydroxybenzoic acid, alkane sulfonic acids, p-toluene sulfonic acid, lower alkyl monocarboxylic acids, oxalic acid, tartaric acid, lactic acid, pyruvic acid, malic acid, succinic acid, gluconic acid and glucuronic acid.
 22. A compound in accordance with claim 21 wherein the said compound is 3-O-3'-(N',N'-dimethylamino-n-propyl)-1,2-O-isopropylidene-D-glucofuranose.
 23. A compound in accordance with claim 22 wherein the said acid is HCl. .Iadd.
 24. A compound having the formula S--O--Y, and therapeutically effective and pharmaceutically acceptable organic acid and inorganic acid salts thereof, wherein S is the residue of a monosaccharide selected from the group consisting of pentoses, hexoses and heptoses which has been derivatized with at least one substance selected from the group consisting of (a) at least one aliphatic alcohol containing 1-18 carbon atoms to produce an ether group at the site of at least one available hydroxyl group, (b) at least one aldehyde containing 1-18 carbon atoms to produce at least one acetal group at the site of at least one available hydroxyl group, (c) at least one ketone containing 1-18 carbon atoms to produce at least one ketal group at the site of at least one available hydroxyl group, and (d) at least one organic acid residue containing 1-18 carbon atoms to produce an ester group at the site of at least one available hydroxyl group, and Y is selected from the group consisting of -(N',N'-dimethylamino-n-propyl), -N',N'-dimethylaminoisopropyl), -(N'-methylpiperidyl), -(N',N'-dimethylaminoethyl), -(2',N',N'-trimethylamino-n-propyl), -(N',N'-dimethylaminomethyl), -(N',N'-dimethylaminopropyl), -(N',N'-dimethylamino-iso-butyl), -(N',N' -dimethylamino-n-butyl), -(N',N'-dimethylamino-iso-pentyl), -(N',N'-dimethylaminopentyl), -(N'-methylamino-n-propyl), -(N'-methyl-N'-ethylamino-n-propyl), -(N',N'-diethylamino-n-propyl), -(N'-ethylamino-n-propyl), -(N'-propylamino-n-propyl), -(N',N'-iso-propylamino-n-propyl), -(1',2'-ethylimino-n-propyl), -(1"-n-propylpyrrolidyl), -(1"-n-propylpiperidyl), -piperidyl, -(N',N'-dimethylamino-sec-butyl), -(methylpiperidyl), -(methylpyrrolidyl) and -(N',N'-dimethylamino-1,2-propenyl). .Iaddend. .Iadd.
 25. A compound according to claim 24 wherein the monosaccharide is a hexose. .Iaddend..Iadd.
 26. A compound according to claim 25 wherein said hexose is glucose. .Iaddend..Iadd.
 27. A compound according to claim 26 wherein said glucose is ethereally monosubstituted at the 1-O- or 6-O-position. .Iaddend..Iadd.
 28. A compound according to claim 27 wherein said glucose is D-glucofuranose. .Iaddend..Iadd.
 29. A compound according to claim 25 wherein said hexose is galactose. .Iaddend..Iadd.
 30. A compound according to claim 29 wherein said galactose is substituted at the 6-O-position. .Iaddend..Iadd.
 31. A compound according to claim 30 wherein said galactose is D-galactopyranose. .Iaddend. 